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| Product | Description | |
|---|---|---|
| Enzyme blend for digesting solid organic materials | An enzyme product consisting of microbes and enzymes used to digest solid organic materials in drains to prevent or treat clogs. Applications: Household. Group: Enzymes. Synonyms: Enzyme blend for digesting solid organic materials; digest solid organic materials; Waste Management Enzymes; digesting; solid organic materials; organic materials. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2714. |  |
| Enzyme blend for treating organic waste | A proprietary enzyme blend that breaks down and solubilizes organic waste, including solids waste in manure pits and food processing plants. Applications: Food handling. Group: Enzymes. Synonyms: treating organic waste; Enzyme blend for treating organic waste; solubilizes organic waste; Waste Management Enzymes; solubilizes; organic waste; Waste Enzymes. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2712. | |
| 1,2,3-Tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D-galactopyranosyl)-b-D-galactopyranoside | 1,2,3-Tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D-galactopyranosyl)-b-D-galactopyranoside is an organic compound used in molecular biology for glycosylation studies. It's crucial in the research of synthesis of antiviral and anticancer drugs targeting glycosyltransferase enzymes. Molecular formula: C61H64O11. Mole weight: 973.15. |  |
| 1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose | 1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose is an organic compound used in biomedical research, particularly in the development of anti-diabetic drugs. It plays a pivotal role in creating inhibitors for the enzyme alpha-glucosidase. Synonyms: α-L-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-; (3aS,5R,6R,6aS)-5-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol; 1-O,2-O:5-O,6-O-Diisopropylidene-alpha-L-glucofuranose. Grades: ≥97%. CAS No. 79943-22-9. Molecular formula: C12H20O6. Mole weight: 260.28. | |
| 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose | 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose is an indispensable compound in the synthesis of antiviral drugs, including Oseltamivir and Zanamivir. These drugs have shown to be effective in treating influenza through their ability to inhibit the neuraminidase enzyme, which in turn hinders the release of new viral fragments from infected cells. The employment of 1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-glucofuranose in the production of antiviral drugs is a prime example of the intersection between organic chemistry and virology, where complex molecules can serve as the backbone for therapeutic interventions. Synonyms: ALPHA.-D-GLUCOFURANOSE, 3-DEOXY-3-FLUORO-1,2-O-(1-METHYLETHYLIDENE)-; SCHEMBL7610553; 1,2-O-ISOPROPYLIDENE-3-DEOXY-3-FLUORO-A-D-GLUCOFURANOSE; WS-00080; D85294; (R)-1-((3aR,5R,6S,6aS)-6-fluoro-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol. Molecular formula: C9H15FO5. Mole weight: 222.21. | |
| 1,3-Diphenyl-4,5-dihydro-1H-pyrazole | 1,3-Diphenyl-4,5-dihydro-1H-pyrazole is a heterocyclic compound belonging to the pyrazole family. It is an organic compound composed of two phenyl rings, a nitrogen atom and a hydrogen atom. Pyrazoles are known for their versatile properties, which makes them useful in a wide range of applications. DPDP is of particular interest due to its potential applications in scientific and medical research. Uses: 1,3-diphenyl-4,5-dihydro-1h-pyrazole is a versatile compound that can be used in a variety of scientific research applications. it has been used as a ligand for the binding of metal ions, such as copper, zinc, and iron, in order to study the structure and function of metalloproteins. it has also been used as a fluorescent probe for the study of enzyme kinetics, as well as for the detection of reac. Group: Heterocyclic organic compound. Alternative Names: 1,3-Diphenylpyrazoline, 1,3-Diphenyl-2-pyrazoline, 2-Pyrazoline, 1,3-diphenyl-, MLS000717825, 1,3-Diphenyl-4,5-dihydro-1H-pyrazole, MolPort-001-631-521, NSC186211, NSC625226, AIDS132054, AIDS-132054, 1,3-Diphenyl-.DELTA.2-pyrazoline, CID302304, ZINC04142401, 1H-Pyrazole, 4,5-dihydro-1,3-diphenyl-, BAS 00363868, SMR000279193, AE-848/30721014, A0944/0044214, 2538-52-5. CAS No. 2538-52-5. Molecular formula: C15H14N2. Mole weight: 222.2851. Purity: 0.96. IUPACName: 2,5-diphenyl-3,4-dihydropyrazole. Canonical SMILES: C1CN(N=C1C2=CC=CC=C2)C3=CC=CC=C3. Densit |  |
| 1H-1,2,4-Triazol-3-amine | 1H-1,2,4-Triazol-3-amine consists of a triazole ring system and an amino group attached to carbon atom 3. The compound has potential applications in various fields such as medicinal chemistry, agrochemicals and material science. In medicinal chemistry, 1H-1,2,4-Triazol-3-amine is used as a starting material for the synthesis of pharmaceutical compounds such as antifungal agents, anticancer agents, and enzyme inhibitors associated with cardiovascular disease. In agrochemicals, it can be used as a raw material for the synthesis of herbicides, fungicides and insecticides. Furthermore, 1H-1,2,4-Triazol-3-amine is used as a ligand in coordination chemistry and as a precursor for the production of new functional materials such as polymers and metal-organic frameworks. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 61-82-5. Pack Sizes: 10 g; 25 g. Product ID: HY-W027592. |  |
| 1L-myo-inositol 1-phosphate cytidylyltransferase | In many organisms this activity is catalysed by a bifunctional enzyme. The cytidylyltransferase domain of the bifunctional EC 2.7.7.74/EC 2.7.8.34 (CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase) is absolutely specific for CTP and 1L-myo-inositol 1-phosphate. The enzyme is involved in biosynthesis of bis(1L-myo-inositol) 1,3'-phosphate, a widespread organic solute in microorganisms adapted to hot environments. Group: Enzymes. Synonyms: CTP:inositol-1-phosphate cytidylyltransferase (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)); IPCT (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phospha. Enzyme Commission Number: EC 2.7.7.74. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3286; 1L-myo-inositol 1-phosphate cytidylyltransferase; EC 2.7.7.74; CTP:inositol-1-phosphate cytidylyltransferase (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)); IPCT (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)); L-myo-inositol-1-phosphate cytidylyltransferase. Cat No: EXWM-3286. | |
| 2,3-Dimethylbutanenitrile | 2,3-Dimethylbutanenitrile is a reactant used in the synthesis of organic compounds as well as in the analysis of enzyme functions and chemical reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 20654-44-8. Pack Sizes: 100mg, 250mg. Molecular Formula: C6H11N, Molecular Weight: 97.16. US Biological Life Sciences. |  Worldwide |
| 2-Acetamido-4,6-O-benzylidene-N-Boc-1,2,5-trideoxy-1,5-imino-D-glucitol | 2-Acetamido-4,6-O-benzylidene-N-Boc-1,2,5-trideoxy-1,5-imino-D-glucitol, a synthetically derived organic compound, serves as a potent inhibitor of glucosidase enzymes in the biomedical sector. In clinical settings, this molecule aids in regulating excessive blood glucose levels in type 2 diabetes patients, in addition to mitigating symptoms of various metabolic disorders. The multifunctional nature of this compound has demonstrated its potential in expanding therapeutic avenues. Molecular formula: C20H28N2O6. Mole weight: 392.45. | |
| 2-O-(2-Nitrophenyl)-a-D-N-acetylneuraminic acid | 2-O-(2-Nitrophenyl)-α-D-N-acetylneuraminic acid, a synthetic organic compound utilized in the biomedical industry, serves as a substrate for sialidase enzymes and acts as a diagnostic tool for detecting sialidosis, an uncommon genetic ailment resulting from sialidase enzyme paucity. Moreover, it plays a pivotal role in the therapeutic drug development for combatting viral infections like influenza and HIV, alongside several malignancies, thus exhibiting substantial clinical significance. The efficaciousness of this compound in multiple biomedical applications remains unparalleled, driving it towards becoming an essential component in the research industry. Synonyms: ONP-a-NeuNAc. CAS No. 157707-92-1. Molecular formula: C17H22N2O11. Mole weight: 430.36. | |
| (2S,3R,4S)-3,4-Dihydroxy-3,4-O-isopropylidene-2,4-di-methyl-pentanal | (2S,3R,4S)-3,4-Dihydroxy-3,4-O-isopropylidene-2,4-di-methyl-pentanal is a complex organic compound used in experimental treatments for metabolic disorders. Its particularly effective in developing drugs essential for regulating enzyme activity linked to diabetes and obesity. Molecular formula: C10H18O3. Mole weight: 186.25. | |
| 3-(Acetylthio)propionic acid | Protected 3-mercaptopropionic acid potentially used as enzyme inhibitor. Group: Heterocyclic organic compound. Alternative Names: S-Acetyl-3-mercaptopropionic acid. CAS No. 41345-70-4. Molecular formula: C5H8O3S. Mole weight: 148.18. Purity: 0.96. IUPACName: 3-acetylsulfanylpropanoic acid. Canonical SMILES: CC(=O)SCCC(O)=O. Density: 1.268g/cm³. Catalog: ACM41345704-1. | |
| 3-hydroxy-2-methylquinolin-4-one 2,4-dioxygenase | Does not contain a metal centre or organic cofactor. Fission of two C-C bonds: 2,4-dioxygenolytic cleavage with concomitant release of carbon monoxide. The enzyme from Arthrobacter sp. can also act on 3-hydroxy-4-oxoquinoline, forming N-formylanthranilate and CO (cf. EC 1.13.11.47, 3-hydroxy-4-oxoquinoline 2,4-dioxygenase), but more slowly. Group: Enzymes. Synonyms: (1H)-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase. Enzyme Commission Number: EC 1.13.11.48. CAS No. 160995-63-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0566; 3-hydroxy-2-methylquinolin-4-one 2,4-dioxygenase; EC 1.13.11.48; 160995-63-1; (1H)-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase. Cat No: EXWM-0566. | |
| 3-hydroxy-4-oxoquinoline 2,4-dioxygenase | Does not contain a metal centre or organic cofactor. Fission of two C-C bonds: 2,4-dioxygenolytic cleavage with concomitant release of carbon monoxide. The enzyme from Pseudomonas putida is highly specific for this substrate. Group: Enzymes. Synonyms: (1H)-3-hydroxy-4-oxoquinoline 2,4-dioxygenase; 3-hydroxy-4-oxo-1,4-dihydroquinoline 2,4-dioxygenase; 3-hydroxy-4(1H)-one, 2,4-dioxygenase; quinoline-3,4-diol 2,4-dioxygenase. Enzyme Commission Number: EC 1.13.11.47. CAS No. 238093-32-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0565; 3-hydroxy-4-oxoquinoline 2,4-dioxygenase; EC 1.13.11.47; 238093-32-8; (1H)-3-hydroxy-4-oxoquinoline 2,4-dioxygenase; 3-hydroxy-4-oxo-1,4-dihydroquinoline 2,4-dioxygenase; 3-hydroxy-4(1H)-one, 2,4-dioxygenase; quinoline-3,4-diol 2,4-dioxygenase. Cat No: EXWM-0565. | |
| 3-Methylglutaric acid | 3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH) [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 626-51-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-113410. | |
| 4-Amino-1-(6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1,3,5-triazin-2(1H)-one | 4-Amino-1-(6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1,3,5-triazin-2(1H)-one is an intriguing organic compound that has been extensively researched in the biomedical industry. The compound displays remarkable potential as a DNA topoisomerase inhibitor, a crucial enzyme involved in DNA replication and cell growth. Its distinctive chemical structure is expected to revolutionize drug discovery and development for the treatment of various cancers and microbial infections. Synonyms: 4-amino-1-[2,3-O-(1-methylethylene)pentofuranosyl]-1,3,5-triazine-2(1H)-one. Grades: 98%. CAS No. 686300-58-3. Molecular formula: C11H16N4O5. Mole weight: 284.27. | |
| 4-Nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-a-D-galactopyranoside | 4-Nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-a-D-galactopyranoside is an organic molecule that plays a vital role in identifying and analyzing carbohydrate-active enzymes, specifically glycosyltransferases. It functions as a substrate in identifying distinct enzymes involved in the degradation of carbohydrates connected to various diseases, such as tuberculosis, bacterial infections, and cancer. It is a critical tool for the scientific community in the field of biochemical research aimed at exploring the intricacies of carbohydrate chemistry and its involvement in pathological processes. Synonyms: 4-Nitrophenyl 2-azido-2-deoxy-a-D-galactopyranoside 3,4,6-triacetate. CAS No. 1147438-51-4. Molecular formula: C18H20N4O10. Mole weight: 452.37. | |
| 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine | 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine (Tetraphenylporphyrin, TPP) is an organic compound that is used in a wide range of scientific research applications. TPP is a macrocyclic ligand with a unique structure and has a variety of properties that make it an ideal molecule for research. TPP is a synthetic molecule that has been used in a variety of research fields, including biochemistry, pharmacology, and materials science. TPP has been used to study the mechanism of action of enzymes, to study the structure and function of proteins, and to study the properties of materials. TPP has also been used in a variety of laboratory experiments, including spectroscopy, crystallography, and microscopy. Uses: Tpp has a variety of scientific research applications. tpp has been used to study the structure and function of proteins, to study the mechanism of action of enzymes, and to study the properties of materials. tpp has also been used in a variety of laboratory experiments, including spectroscopy, crystallography, and microscopy. tpp has also been used in the study of the structure and function of dn. Group: Nitrogen-donor ligands. Alternative Names: 5,10,15,20-Tetrakis(4-butoxyphenyl)-21H,23H-Porphine. CAS No. 57450-62-1. Molecular formula: C60H62N4O4. Mole weight: 903.2 g/mol. Purity: 0.98. IUPACName: 5,10,15,20-tetrakis(4-butoxyphenyl)-21,23-dihydroporphyrin. Canonical SMILES: CCCCOC1=CC=C (C=C1 | |
| 5,12-Bis(phenylethynyl)naphthacene | 5,12-Bis(phenylethynyl)naphthacene (5,12-BPEN) is a synthetic organic compound belonging to the class of naphthalene derivatives. It is a derivative of naphthalene and is composed of two phenylethynyl groups connected to a central naphthalene ring. 5,12-BPEN has been studied extensively for its potential applications in scientific research and has been found to have a range of biochemical and physiological effects. b experiments, and its potential future directions. Uses: 5,12-bis(phenylethynyl)naphthacene has been studied extensively for its potential applications in scientific research. it has been used in the study of the structure and function of proteins, as well as in the study of the interactions between proteins and other molecules. it has also been used in the study of dna and rna, as well as in the study of the structure and function of cells. additionally, 5,12-bis(phenylethynyl)naphthacene has been used in the study of the role of lipids in cell membranes and in the study of the role of enzymes in metabolic pathways. Alternative Names: 5,12-Bis(phenylethynyl)tetracene. CAS No. 18826-29-4. Molecular formula: C34H20. Mole weight: 428.5. Appearance: White to Off-White powder. Purity: 0.98. Canonical SMILES: C1=CC=C (C=C1)C#CC2=C3C=CC=CC3=C (C4=CC5=CC=CC=C5C=C42)C#CC6=CC=CC=C6. Density: 1.25 g/mL. ECNumber: 242-605-4. Catalog: ACM18826294. | |
| 6-Deoxy-d-gulose | 6-Deoxy-D-gulose, a paramount biomedical compound, unveils its true potential in unraveling carbohydrate synthesis intricacies, offering profound insights into varied metabolic pathways. Its prowess extends to suppressing glucose metabolism-associated enzymes, warranting its therapeutic value in thwarting cancer and diabetes. Group: Heterocyclic organic compound. CAS No. 5158-61-2. Catalog: ACM5158612. | |
| 6-Methoxy-2-naphthalene carboxaldehyde | 6-Methoxy-2-naphthalene carboxaldehyde is used as a diagnostic reagent in tumor studies involving aldehyde dehydrogenase enzymes. In addition it is used in organic synthesis reactions forming fluorescent substrates for inhibition studies relating to hypertension and vascular inflammation. Group: Biochemicals. Alternative Names: 2-Methoxy-6-naphthalene carboxaldehyde; 6-Methoxy-2-naphthaldehyde; 6-Methoxy-2-naphthalene carboxaldehyde; MONAL 62. Grades: Highly Purified. CAS No. 3453-33-6. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| Acetoxyacetic acid | Acetoxyacetic acid (CAS# 13831-30-6) is a versatile organic building block, used in the synthesis of pharmaceutical compounds, including inhibitors and therapeutic agents. It can be used for the synthesis of analogs of 5-Aminolevulinic Acid, which are potential inhibitors of ALA dehydratase (porphobilinogen synthase), an early enzyme of tetrapyrrole biosynthesis. Synonyms: 2-acetyloxyacetic acid. CAS No. 13831-30-6. Molecular formula: C4H6O4. Mole weight: 118.09. | |
| Adenosine5'-(trihydrogen diphosphate),1-b-D-ribofuranosyl-,intramol. p',5''-ester | Heterocyclic Organic Compound. Alternative Names: cyclic adenosine 5-diphosphoribose; Cyclic Adenosine Diphosphate Ribose; cADP-Ribose; Cyclic ADPR; cyclic ADP-D-ribose; E-NAD; Enzyme-activated NAD; cyclic adenosine 5-diphosphate ribose; cADPR; adenosine 5-cyclic-diphosphoribose. CAS No. 119340-53-3. Molecular formula: C15H21N5O13P2. Mole weight: 541.3005. Appearance: Lyophilized powder. Purity: >94%. IUPACName: cyclic ADP-ribose. Density: 2.57 g/cm³. Catalog: ACM119340533. | |
| Albumin | Albumin. CAS No. 9048-49-1. Product ID: PE-0600. Category: Stabilizer; Therapeutic Agents. Product Keywords: Other Materials; Stabilizers; PE-0600; Albumin; Stabilizer; Therapeutic Agents; ; 9048-49-1. Chemical Name: Serum albumin. Grade: Pharmceutical Excipients. Administration route: Intravenous. Dosage Form: Intravenous injection. Stability and Storage Conditions: Albumin is a protein and is therefore prone to chemical degradation and denaturation under extreme pH conditions, high salt concentrations, heat, enzymes, organic solvents and other chemical agents present. Albumin solution should be stored away from light at 2 ~ 25 ° C, or according to label instructions. Source and Preparation: Human blood albumin is a sterile, pyrogen free serum albumin product obtained from a healthy donor's isolate (source blood, plasma, serum or placenta); The source material must not be tested to contain hepatitis B surface antigen. The production process should ensure that the product is safe and can be used for intravenous injection. Applications: Albumin is mainly used as an excipient in the prescription of injectable drugs, as a stabilizer for proteins and enzymes in the prescription. Albumin is also used in the preparation of microspheres and microcapsules in experimental drug delivery systems. As a stabilizer, albumin is used in protein prescriptions at a low concentration of 0.003%. However, concentrations of 1.to 5% are usually |  |
| Alginic Acid Calcium Salt | Calcium alginate is a water-insoluble, gelatinous, cream-coloured substance that can be created through the addition of aqueous calcium chloride to aqueous sodium alginate. Calcium alginate is also used for entrapment of enzymes and forming artificial seeds in plant tissue culture.Alginate is the term usually used for the salts of alginic acid, but it can also refer to all the derivatives of alginic acid and alginic acid itself; in some publications the term algin is used instead of alginate. Alginate is present in the cell walls of brown algae as the calcium, magnesium and sodium salts of alginic acid. Group: Heterocyclic organic compound. Alternative Names: Sodium alginate, Landalgine, Nouralgine, Pectalgine, Algiline, Calginate, Combinace, Duckalgin, Kaltostat, Kelcosol, Protanal, Protatek, Amnucol, Halltex, Kelacid, Kelsize, Keltone, Lamitex, Manucol, Manutex. CAS No. 9005-35-0. Molecular formula: C36H42Ca3O36. Mole weight: 398.316680 [g/mol]. Appearance: Gelatinous, cream coloured substance. Purity: 0.96. IUPACName: 6-(2-carboxy-4,5-dihydroxy-6-methoxyoxan-3-yl)oxy-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid. Catalog: ACM9005350. | |
| Ancymidol | Ancymidol is an anti-gibberellin and can inhibit ornamental plant growth. Uses: Ancymidol is a plant growth retardant. it inhibits the oxidation of ent-kaurene, an enzyme that interferes with the biosynthesis of gibberellins. it has been reported that plant treated with ancymidol has a dwarf-like appearance due to the reductions of internodes elongation. Group: Heterocyclic organic compound. Alternative Names: α-Cyclopropyl-α-[4-methoxyphenyl]-5-pyrimidinemethanol. CAS No. 12771-68-5. Molecular formula: C15H16N2O2. Mole weight: 256.3 g/mol. Appearance: White to Yellow Powder. Catalog: ACM12771685. | |
| aryl sulfotransferase | A number of aromatic compounds can act as acceptors. Organic hydroxylamines are not substrates (cf. EC 2.8.2.9 tyrosine-ester sulfotransferase). Group: Enzymes. Synonyms: phenol sulfotransferase; sulfokinase; 1-naphthol phenol sulfotransferase; 2-naphtholsulfotransferase; 4-nitrocatechol sulfokinase; arylsulfotransferase; dopamine sulfotransferase; p-nitrophenol sulfotransferase; phenol sulfokinase; ritodrine sulfotransferase; PST. Enzyme Commission Number: EC 2.8.2.1. CAS No. 9026-9-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3368; aryl sulfotransferase; EC 2.8.2.1; 9026-09-9; phenol sulfotransferase; sulfokinase; 1-naphthol phenol sulfotransferase; 2-naphtholsulfotransferase; 4-nitrocatechol sulfokinase; arylsulfotransferase; dopamine sulfotransferase; p-nitrophenol sulfotransferase; phenol sulfokinase; ritodrine sulfotransferase; PST. Cat No: EXWM-3368. | |
| Betaine | Betaine, is the product of the enzyme oxidation of choline. It can also be used as an organic osmolytes. Betain is a methyl donor of increasingly recognized significance in biology. It can also be used for the treatment of homocystinuria which is an inherited disorder of the metabolism of amino acid methionine. Group: Biochemicals. Alternative Names: 1-Carboxy-N,N,N-trimethyl-Methanaminium Inner Salt; (Carboxymethyl) trimethylammonium Hydroxide Inner Salt; (Trimethylammonio) acetate; Abromine; Aminocoat; Aquadew AN 100; Betafin; Betafin BCR; Betafin BP; Betafin BP 20; Cystadane; Fencaijian; FinnStim; Glycine Betaine; Trimethylbetaine Glycine; Glycocoll Betaine; Glycylbetaine; Greenstim; Loramine AMB 13; Lycine; N,N,N-Trimethylglycine; Oxyneurine; Rubrine C; Trimethylbetaine; Trimethylglycocoll; α-Earleine. Grades: Highly Purified. CAS No. 107-43-7. Pack Sizes: 100g, 250g, 500g. Molecular Formula: C?H??NO?, Molecular Weight: 117.15. US Biological Life Sciences. | Worldwide |
| β-NADH, Reduced Disodium Salt (Nicotinamide Adenine Dinucleotide) | Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron tran...accomplished by the removal of hydrogen atoms. Both of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. Group: Biochemicals. Alternative Names: β-DPNH; β-NADH; DPNH; Diphosphopyridine nucleotide, reduced form; NADH. Grades: Highly Purified. CAS No. 606-68-8. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C21H27N7O14P2Na2, Molecular Weight: 709.41. US Biological Life Sciences. | Worldwide |
| Bilirubin | Bilirubin (formerly referred to as haematoidin) is a yellow compound that occurs in the normal catabolic pathway that breaks down heme in vertebrates. This catabolism is a necessary process in the bodys clearance of waste products that arise from the destruction of aged red blood cells. First the hemoglobin gets stripped of the heme molecule which thereafter passes through various processes of porphyrin catabolism, depending on the part of the body in which the breakdown occurs. For example, the molecules excreted in the urine differ from those in the feces. The production of biliverdin from heme is the first major step in the catabolic pathway, after which the enzyme biliverdin reductase performs the second step, producing bilirubin from biliverdin.Bilirubin is excreted in bile and urine, and elevated levels may indicate certain diseases. It is responsible for the yellow color of bruises and the yellow discoloration in jaundice. Its subsequent breakdown products, such as stercobilin, cause the brown color of feces. A different breakdown product, urobilin, is the main component of the straw-yellow color in urine.It has also been found in plants. Group: Heterocyclic organic compound. Alternative Names: Cholerythrin. CAS No. 635-65-4. Molecular formula: C33H36N4O6. Mole weight: 584.66. Appearance: Solid. Purity: 0.98. IUPACName: 3-[2-[[3-(2-Carboxyethyl)-5-[(Z)-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol- | |
| Bromelain | Bromelain is a protein-digesting enzyme extracted from the stem, fruit, and juice of the pineapple plant (Ananas comosus). It belongs to a group of enzymes called proteases or proteinases. Bromelain is a complex mixture of enzymes that can hydrolyze (break down) various types of proteins, including collagen, elastin, and fibrin. Uses: 1. anti-inflammatory: bromelain has been found to possess anti-inflammatory properties, which makes it useful in the treatment of arthritis, asthma, allergies, and other conditions characterized by inflammation. 2. digestive aid: bromelain is often used as a digestive aid because it helps break down proteins in the digestive tract, aiding digestion and reducing bloating. 3. wound healing: bromelai. Group: Heterocyclic organic compound. Alternative Names: STEM BROMELAIN; 3.4.22.32; BROMELAIN; BROMELAIN PINEAPPLE;BROMELIN;EC 3.4.22.1;EC 3.4.22.32;EC 3.4.22.4. CAS No. 9001-00-7. Molecular formula: N/A. Mole weight: N/A. Appearance: yellow to beige crystalline powder. Catalog: ACM9001007. | |
| bromide peroxidase | Bromoperoxidases of red and brown marine algae (Rhodophyta and Phaeophyta) contain vanadate. They catalyse the bromination of a range of organic molecules such as sesquiterpenes, forming stable C-Br bonds. Bromoperoxidases also oxidize iodides. Group: Enzymes. Synonyms: bromoperoxidase; haloperoxidase (ambiguous); eosinophil peroxidase. Enzyme Commission Number: EC 1.11.1.18. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0499; bromide peroxidase; EC 1.11.1.18; bromoperoxidase; haloperoxidase (ambiguous); eosinophil peroxidase. Cat No: EXWM-0499. | |
| Cadp-ribose | Heterocyclic Organic Compound. Alternative Names: cyclic adenosine 5-diphosphoribose; Cyclic Adenosine Diphosphate Ribose; cADP-Ribose; Cyclic ADPR; cyclic ADP-D-ribose; E-NAD; Enzyme-activated NAD; cyclic adenosine 5-diphosphate ribose; cADPR; adenosine 5-cyclic-diphosphoribose. CAS No. 119340-53-5. Molecular formula: C15H21N5O13P2. Mole weight: 541.3. Appearance: Lyophilized powder. Purity: 0.96. IUPACName: cyclic ADP-ribose. Density: 2.57 g/cm³. Catalog: ACM119340535. | |
| catalase | A hemoprotein. A manganese protein containing MnIII in the resting state, which also belongs here, is often called pseudocatalase. The enzymes from some organisms, such as Penicillium simplicissimum, can also act as a peroxidase (EC 1.11.1.7) for which several organic substances, especially ethanol, can act as a hydrogen donor. Enzymes that exhibit both catalase and peroxidase activity belong under EC 1.11.1.21, catalase-peroxidase. Group: Enzymes. Synonyms: equilase; caperase; optidase; catalase-peroxidase; CAT. Enzyme Commission Number: EC 1.11.1.6. CAS No. 9001-5-2. CAT. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0508; catalase; EC 1.11.1.6; 9001-05-2; equilase; caperase; optidase; catalase-peroxidase; CAT. Cat No: EXWM-0508. | |
| CDP-L-myo-inositol myo-inositolphosphotransferase | In many organisms this activity is catalysed by a bifunctional enzyme. The di-myo-inositol-1,3'-phosphate-1'-phosphate synthase domain of the bifunctional EC 2.7.7.74/EC 2.7.8.34 (CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase) uses only 1L-myo-inositol 1-phosphate as an alcohol acceptor, but CDP-glycerol, as well as CDP-1L-myo-inositol and CDP-D-myo-inositol, are recognized as alcohol donors. The enzyme is involved in biosynthesis of bis(1L-myo-inositol) 1,3-phosphate, a widespread organic solute in microorganisms adapted to hot environments. Group: Enzymes. Synonyms: CDP-inositol:inositol-1-phosphate transferase (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)); DIPPS . Enzyme Commission Number: EC 2.7.8.34. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3333; CDP-L-myo-inositol myo-inositolphosphotransferase; EC 2.7.8.34; CDP-inositol:inositol-1-phosphate transferase (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)); DIPPS (bifunctional CTP:inositol-1-phosphate cytidylyltransferase/CDP-inositol:inositol-1-phosphate transferase (IPCT/DIPPS)). Cat No: EXWM-3333. | |
| chloride peroxidase | Brings about the chlorination of a range of organic molecules, forming stable C-Cl bonds. Also oxidizes bromide and iodide. Enzymes of this type are either heme-thiolate proteins, or contain vanadate. A secreted enzyme produced by the ascomycetous fungus Caldariomyces fumago (Leptoxyphium fumago) is an example of the heme-thiolate type. It catalyses the production of hypochlorous acid by transferring one oxygen atom from H2O2 to chloride. At a separate site it catalyses the chlorination of activated aliphatic and aromatic substrates, via HClO and derived chlorine species. In the absence of halides, it shows peroxidase (e.g. phenol oxidation) and peroxygenase activities. The latter ...peroxidase, and is related to bromide peroxidase (EC 1.11.1.18). It contains vanadate and oxidizes chloride, bromide and iodide into hypohalous acids. In the absence of halides, it peroxygenates organic sulfides and oxidizes ABTS [2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)] but no phenols. Group: Enzymes. Synonyms: chloroperoxidase; CPO; vanadium haloperoxidase. Enzyme Commission Number: EC 1.11.1.10. CAS No. 9055-20-3. CPO. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0491; chloride peroxidase; EC 1.11.1.10; 9055-20-3; chloroperoxidase; CPO; vanadium haloperoxidase. Cat No: EXWM-0491. | |
| cis-4-Hydroxy-L-proline | Hydroxyprolines are valuable chiral building blocks for organic synthesis of pharmaceuticals. Several microorganisms producing proline trans-4- and cis-3-hydroxylase were discovered and these enzymes were applied to the industrial production of trans-4- and cis-3-hydroxy-L-proline. Group: Biochemicals. Alternative Names: (4S)-4-Hydroxy-L-proline; (2S,4S)-4-Hydroxyproline; (S)-Allo-hydroxyproline; (2S,4S)-4-Hydroxypyrrolidine-2-carboxylic Acid; L-Allohydroxyproline; cis-4-Hydroxyproline; cis-Hydroxyproline. Grades: Highly Purified. CAS No. 618-27-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Concentrated alkaline protease for Medical | Concentrated, alkaline protease enzyme used in medical and surgical instrument cleaning products to remove protein-containing, organic materials such as blood, mucus, feces and foods. Applications: Laundry. Group: Enzymes. Synonyms: alkaline protease; Concentrated alkaline protease for Medical; alkaline protease enzyme; medical; surgical instrument ; cleaning; Detergents; Concentrated alkaline protease for Medical; DETE-2631. CAS No. 37259-58-8. Alkaline Protease. Appearance: powder or liquid. alkaline protease; Concentrated alkaline protease for Medical; alkaline protease enzyme; medical; surgical instrument ; cleaning; Detergents; Concentrated alkaline protease for Medical; DETE-2631. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: DETE-2631. | |
| Corey lactone THP | Corey lactone THP, being an organic compound, has proven to be an essential building block in synthesizing several drugs, distinguishedly an antitumor agent and an angiotensin-converting enzyme inhibitor. Additionally, it finds its application as a safeguarding group for alcohols during organic synthesis. Its utilization in these domains is of critical significance owing to its potential in enhancing drug efficacy. Synonyms: (3aR,4S,5R,6aS)-4-(Hydroxymethyl)-5-((tetrahydro-2H-pyran-2-yl)oxy)hexahydro-2H-cyclopenta[b]furan-2-one; 2H-Cyclopenta[b]furan-2-one, hexahydro-4-(hydroxymethyl)-5-[(tetrahydro-2H-pyran-2-yl)oxy]-, (3aR,4S,5R,6aS)-. Grades: 95%. CAS No. 69222-61-3. Molecular formula: C13H20O5. Mole weight: 256.29. | |
| Cyclodextrins | Cyclodextrins occur as white, practically odorless, fine crystalline powders, having a slightly sweet taste. Some cyclodextrin derivatives occur as amorphous powders. Synonyms: Cavitron; cyclic oligosaccharide; cycloamylose; cycloglucan; Encapsin; Schardinger dextrin. Product ID: PE-0591. Category: Solubilizing Agents; Stabilizing Agents. Product Keywords: Stabilizers; Solubilizer Excipients; PE-0591; Cyclodextrins; Solubilizing Agents; Stabilizing Agents;. UNII: Z1LH97KTRM. Grade: Pharmceutical Excipients. Administration route: α-cyclodextrin (injection); β-cyclodextrin (oral; topical); γ-cyclodextrin (IV injections). Dosage Form: α-cyclodextrin (injection preparations); β-cyclodextrin (oral tablets, topical gels); γ-cyclodextrin (IV injections). Stability and Storage Conditions: β-Cyclodextrin and other cyclodextrins are stable in the solid state if protected from high humidity. Cyclodextrins should be stored in a tightly sealed container, in a cool, dry place. Source and Preparation: Cyclodextrins are manufactured by the enzymatic degradation of starch using specialized bacteria. For example, b-cyclodextrin is produced by the action of the enzyme cyclodextrin glucosyltransferase upon starch or a starch hydrolysate. An organic solvent is used to direct the reaction that produces b-cyclodextrin, and to prevent the growth of microorganisms during the enzymatic reaction. The inso | |
| Cyclopropylamine | It can inactivate major human drug-metabolizing cytochromes P450 enzymes. Group: Heterocyclic organic compound. Alternative Names: c-propyl amine;cyclopropyl-amine;cyclopropylNH2. CAS No. 765-30-0. Molecular formula: C3H7N. Mole weight: 57.09. Appearance: Clear liquid. Density: 0.824. Catalog: ACM765300. | |
| Cystamine dihydrochloride | Cystamine dihydrochloride is the dihydrochloride salt of cystamine, which is an organic disulfide that inhibits tissue transglutaminase (TGM2) with an IC50 value of approximately 2.5 mM. It is orally available, and decreases aggregated and cross-linked huntingtin in transfected cells. It is neuroprotective in mouse models of Huntington's disease. It has exhibited suppressive effects against HIV replication in infected human cells. It could extend survival and improve motor performance in transgenic HD mice. It inhibits caspase 3, increases intracellular glutathione, and reduces inflammation in a rat model of inflammatory bowel disease. Uses: Enzyme inhibitors. Synonyms: 2-(2-aminoethyldisulfanyl)ethanamine; dihydrochloride. Grades: > 97 %. CAS No. 56-17-7. Molecular formula: C4H14Cl2N2S2. Mole weight: 225.20. | |
| Diethylenetriamine-pentaacetic acid pentasodium salt solution | Diethylenetriamine-pentaacetic acid pentasodium salt solution. Synonyms: DTPA Na5. CAS No. 140-01-2. Product ID: CDC10-0104. Molecular formula: C14H24N3NaO10. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Diethylenetriamine-pentaacetic acid pentasodium salt solution; CDC10-0104; 140-01-2; C14H24N3NaO10; DTPA Na5; MFCD00051016; 140-01-2. Purity: ~40% in H2O. Color: Clear. Physical State: Solution. Quality Level: 100. Application: Diethylenetriamine-pentaacetic acid pentasodium salt solution may be used in a competitive indirect enzyme-linked immunoassay for the quantitative measurement of lead ions. It may be used in one-step immunochromatographic assay (ICA) for the fast detection of lead ions in water samples. Boiling Point: 106 °C. Melting Point: -40 °C. Density: 1.29 g/cm3. Product Description: Diethylenetriamine-pentaacetic acid pentasodium salt is an organic chelating agent. | |
| Dimethyl dicarbonate | Dimethyl dicarbonate (DMDC) is an organic compound which is a Colorless liquid with a sharp odor at room temperature. It is primarily used as a beverage preservative, processing aid, or sterilant (INS No. 242), and acts by inhibiting the enzymes acetate kinase and L-glutamic acid decarboxylase. It has also been proposed that DMDC inhibits the enzymes alcohol dehydrogenase and glyceraldehyde 3-phosphate dehydrogenase by causing the methoxycarbonylation of their histidine components. Group: Heterocyclic organic compound. Alternative Names: methoxycarbonyl methyl carbonate;DMPC Dimethyl pyrocarbonate Pyrocarbonic acid dimethyl ester. CAS No. 4525-33-1. Molecular formula: C4H6O5. Mole weight: 134.09. IUPACName: methoxycarbonyl methyl carbonate. Canonical SMILES: COC(=O)OC(=O)OC. Density: 1.242 g/cm³. Catalog: ACM4525331. | |
| Enzyme blend for flour proteins | This food-grade , non-synthetic, and organic-certifiable enzyme blend is used to hydrolyze soya, pea, yeast, maize and wheat flour proteins, producing high-quality functional protein hydrolysates. Applications: Vegetable proteins. Group: Enzymes. Enzyme for flour proteins. Appearance: powder or liquid. for flour proteins; Vegetable Proteins enzyme; hydrolyze soya enzyme;hydrolyze pea enzyme; hydrolyze yeast enzyme; maize and wheat flour proteins; pea; maize; wheat; hydrolyze soya; hydrolyze; Enzyme blend for flour proteins; PRO-1825. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: PRO-1825. | |
| Enzyme blend for hydrolyzing animal source proteins | This food-grade, non-synthetic, and organic-certifiable enzyme blend is used to hydrolyze fish, poultry, milk, gelatin, and other animal source proteins, producing high-quality functional protein hydrolysates. Applications: Meat & fish proteins. Group: Enzymes. Enzymes of animimal source proteins. Appearance: powder or liquid. hydrolyzing; animal source proteins; Meatand Fish Proteins enzyme; organic-certifiable; producing high-quality functional protein; hydrolysates enzyme; Enzyme blend for hydrolyzing animal source proteins; PRO-1822. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: PRO-1822. | |
| Enzyme blend for treating horse waste products | A blend of , enzymes, plant extracts and buffers,designed to eliminate accumulated ammonia, hydrogen sulfide and other volatile organic compounds arising from horse waste products. Applications: Animal. Group: Enzymes. Synonyms: treating horse waste products; horse waste products; elimination of accumulated ammonia; hydrogen sulfide; volatile organic compounds; Waste Management Enzymes; treating horse waste; elimination ammonia; elimination; horse waste; waste; Enzyme blend for treating horse waste products. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2718. | |
| Enzyme blend for treating septic tanks | A blend of naturally microbes, enzymes, plant extracts and buffers for the digestion of solid waste and elimination of odors in septic tanks and portable toilets. Applications: Organic waste. Group: Enzymes. Synonyms: treating septic tanks; enzyme for solid waste; odors in septic tanks and portable toilets; Waste Management Enzymes; solid; portable toiletswaste; tanks; odors in septic; odors; Enzyme blend for treating septic tanks. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2720. | |
| Enzyme blend for treating sewage | A blend of enzymes and bioenhancers for effluent/sewage treatment. Applications: Organic waste. Group: Enzymes. Synonyms: for treating sewage; sewage treatment; Waste Management Enzymes; Enzyme blend for treating sewage. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2722. | |
| Enzyme blend used in wastewater | It helps reduce costs in removing sludge by the digestive action of select bacteria and enzymes,designd for use in industrial wastewater treatment plants. Applications: Organic waste. Group: Enzymes. Synonyms: for waste water; enzyme for industrial waste water; Waste Management Enzymes; waste water; industrial wastewater; Enzyme blend used in wastewater. Waste Management. Appearance: inquire. digesting waste oils; digest grease?fats and oils; Waste Management Enzymes; digesting; digesting waste oils; waste oils. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: WME-2721. | |
| Flurprimidol | Flurprimidol is known as a growth retardant containing an N-containing heterocycle. It functions by inhibiting cytochrome P450-dependent monooxygenases, which are enzymes that catalyzes the oxidation of ent-kaurene into ent-kaurene acid, thus it inhibits the gibberellin biosynthesis which leads to the inhibition of internodes elongation. Uses: Flurprimidol not only works to retard plant growth, but also helps enhance bulb formation. it has been reported that treatment of shallot bulbs with 10 um flurprimidol increase bulb formations with no effect on division rate. Group: Heterocyclic organic compound. Alternative Names: ALPHA- (1-METHYLETHYL)-ALPHA-[4- (TRIFLUOROMETHOXY)PHENYL]-5-PYRIMIDINEMETHANOL. CAS No. 56425-91-3. Molecular formula: C15H15F3N2O2. Mole weight: 312.29 g/mol. Appearance: White to Off-White Powder. Catalog: ACM56425913. | |
| Glucoamylase for Alcohol Industry | Glucoamylase adopts fine microorganisms of aspergillus niger extract from its submerged fermentation, no transglucosidase and with high percent conversion. This series products have two kinds-powder and liquid, be widely used in starch sugar,alcohol,brewage,monosodium glutamate,glucose, organic acid, bacteriophage and other industries. Applications: Starch sugar,alcohol,brewage. Group: Enzymes. Synonyms: Glucoamylase for Alcohol Industry; Glucoamylase; High-percent Conversion; Glucoamylase; Alcohol Enzyme; Alcohol; Glucoamylase for Alcohol Industry; ALC-1516. CAS No. 9032-08-0. Glucoamylase. Appearance: powder or liquid. Source: Aspergillus niger. Glucoamylase for Alcohol Industry; Glucoamylase; High-percent Conversion; Glucoamylase; Alcohol Enzyme; Alcohol; Glucoamylase for Alcohol Industry; ALC-1516. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: ALC-1516. | |
| Hexokinase-1 from Human, Recombinant | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Hk1 human recombinant produced in e. coli is a single, non-glycosylated, polypeptide chain fused to his tag a...ferase; EC 2.7.1.1; 9001-51-8. Enzyme Commission Number: EC 2.7.1.1. CAS No. 9001-51-8. Purity: Greater than 95.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. Hexokinase. Mole weight: 104.6 kDa. Activity: 7-8 units/ml. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please avoid freeze-thaw cycles. Appearance: Sterile filtered colorless solution. Source: E. coli. Species: Human. Hexokinase-1; EC 2.7.1.1; Hexokinase type I; HK I; Brain form hexokinase; HK1-ta; HK1-tb; HXK1; HK1. Cat No: NATE-0844. | |
| Hexokinase-2 from Human, Recombinant | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Hk2 human recombinant produced in e. coli is a single, non-glycosylated, polypeptide chain fused to his tag a...rase; EC 2.7.1.1; 9001-51-8. Enzyme Commission Number: EC 2.7.1.1. CAS No. 9001-51-8. Purity: Greater than 90.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. Hexokinase. Mole weight: 104.1 kDa. Activity: 3-4 units/ml. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please avoid freeze-thaw cycles. Appearance: Sterile filtered colorless solution. Source: E. coli. Species: Human. Hexokinase-2; EC 2.7.1.1; HK2; Hexokinase type II; HK II; Muscle form hexokinase; HXK2; DKFZp686M1669. Cat No: NATE-0845. | |
| Hexokinase-3 from Human, Recombinant | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Hk-3 human recombinant produced in e. coli is a single, non-glycosylated, polypeptide chain fused to his tag ...phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase; EC 2.7.1.1; 9001-51-8. Enzyme Commission Number: EC 2.7.1.1. CAS No. 9001-51-8. Purity: Greater than 95.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. Hexokinase. Mole weight: 101.1 kDa. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please avoid freeze-thaw cycles. Appearance: Sterile filtered colorless solution. Source: E. coli. Species: Human. Hexokinase-3; EC 2.7.1.1; Hexokinase type III; HK III; HXK3; HK3. Cat No: NATE-0846. | |
| Hexokinase-4 from Human, Recombinant | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Glucokinase human recombinant produced in e. coli is a single, non-glycosylated, polypeptide chain fused to h...se; hexokinase; ATP:D-hexose 6-phosphotransferase; EC 2.7.1.1; 9001-51-8. Enzyme Commission Number: EC 2.7.1.2. CAS No. 9001-36-9. Purity: Greater than 95.0% as determined by SDS-PAGE. Hexokinase. Mole weight: 54.3 kDa. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please avoid freeze-thaw cycles. Appearance: Sterile filtered colorless solution. Source: E. coli. Species: Human. Glucokinase; EC 2.7.1.2; Hexokinase-4; Hexokinase type IV; HK IV; HK4; Hexokinase-D; GCK; GK; GLK; HHF3; HKIV; HXKP; MODY2. Cat No: NATE-0847. | |
| Hexokinase from Kluyveromyces fragilis, Recombinant | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Group: Enzymes. Synonyms: hexokinase (phosphorylating); ATP-dependent hexokinase; glucose ATP phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase; EC 2.7.1.1. Enzyme Commission Number: EC 2.7.1.1. CAS No. 9001-51-8. Hexokinase. Mole weight: 54 Kd (SDS-PAGE). Activity: > 150 Units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Kluyveromyces fragilis. hexokinase (phosphorylating); ATP-dependent hexokinase; glucose ATP phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase; EC 2.7.1.1. Cat No: NATE-1034. | |
| Hexokinase from Yeast, chemically modified | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Recombinant enzyme that converts hexose to hexose-6-phosphate. take advantage of the improved stability in liquid reagents. rely on the proven diagnostic quality of this product. Applications: Use hexokinase in diagnostic tests for blood glucose using the hexokinase method and for the determination of creatine kinase. Group: Enzymes. Synonyms: hexokinase type . Hexokinase. Mole weight: 57 kD (SDS-PAGE). Activity: > 40 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 18 months. Store dry. Appearance: White lyophilizate. Source: Yeast. hexokinase type IV glucokinase; hexokinase D; hexokinase type IV; hexokinase (phosphorylating); ATP-dependent hexokinase; glucose ATP phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase. Cat No: NATE-0989. | |
| Immobilized Lipase B from Candida antarctica, Recombinant | Recombinant Lipase B from Candida antarctica (CALB) is produced by submerged fermentation with genetically modified Pichia pastoris. CALB can be used in the water phase or organic phase catalytic esterification, esterolysis, transesterification, ring opening polyester synthesis, aminolysis, hydrolysis of amides, acylation of amines and addition reaction. CALB is with high chiral selectivity and position selectivity, so it can be widely used in oil processing, food, medicine, cosmetic and other chemical industries.CALB is immobilized by physical adsorption on the highly hydrophobic resin that is a macroporous, styrene/methacrylate polymer. Applications: Immobilized calb is suitable for applications in organic solvents and solvent-free systems, and can be recycled and reused for much times in suitable conditions. Group: Enzymes. Synonyms: Lipase B; Immobilized Lipase B; Immobilized CALB; CALB; Immobilized Lipase; Immobilized; Lipase. Lipase. Source: Pichia pastoris. Species: Candida antarctica. Lipase B; Immobilized Lipase B; Immobilized CALB; CALB; Immobilized Lipase; Immobilized; Lipase. Cat No: NATE-1897. | |
| Immobilized Lipase from Pseudomonas sp. | A lipase is an enzyme that catalyzes the hydrolysis of fats (lipids). Lipases are a subclass of the esterases. Lipases perform essential roles in the digestion, transport and processing of dietary lipids (e.g. triglycerides, fats, oils) in most, if not all, living organisms. Genes encoding lipases are even present in certain viruses. The enzyme is a preparation of a pseudomonas sp. lipase (dia-210) immobilized on hyflo super-cel. Applications: This enzyme is useful for enzymatic ester synthesis, transesterification, acidolysis and alcholysis in organic solvents or solvent free substrate. Group: Enzymes. Synonyms: immobilized Lipase; Lipase; Lipase, immobilized Lipase. Lipase. Activity: 0.5U/mg-solid or more. Appearance: Light brown powder (immobilized on Hyflo Super-Cel). Source: Pseudomonas sp. immobilized Lipase; Lipase; Lipase, immobilized Lipase. Cat No: DIA-277. | |
| KT 5926 | KT 5926, an organic heterooctacyclic compound, selectively inhibits nerve growth factor-dependent neurite elongation. Uses: Enzyme inhibitors. Synonyms: 9-hydroxy-9-methoxycarbonyl-8-methyl-14-n-propoxy-2, 3, 9, 10-tetrahydro-8, 11-epoxy-1H, 8H, 11H-2, 7b, 11a-triazadibenzo(a, g)cycloocta[cde]trinden-1-on; KT5926; KT-5926; KT 5926. CAS No. 126643-38-7. Molecular formula: C30H27N3O6. Mole weight: 525.55. | |
| Lipase B from Candida Antarctica, Recombinant | Lipase B from Candida antarctica has been shown to be an effective catalyst for the synthesis of esters of ethyl D-glucopyranoside from fatty acids larger than octanoic acid. It has also been found to catalyze a wide variety of organic reactions including many different regio-and enantio-selective syntheses. Applications: Lipases are used industrially for the resolution of chiral compounds and the transesterification production of biodiesel. Group: Enzymes. Synonyms: EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; t. Enzyme Commission Number: EC 3.1.1.3. CAS No. 9001-62-1. Lipase. Activity: ~9 units/mg. Storage: 2-8°C. Form: powder, beige. Source: Aspergillus oryzae. Species: Candida Antarctica. EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; tributyrinase; Tween hydrolase; steapsin; triacetinase; tributyrin esterase; Tweenase; amno N-AP; Takedo 1969-4-9; Meito MY 30; Tweenesterase; GA 56; capalase L; triglyceride hydrolase; triolein hydrolase; tween-hydrolyzing esterase; amano CE; cacordase; triglyceridase; triacylglycerol ester hydrolase; amano P; amano AP; PPL; glycerol-ester hydrolase; GEH; meito Sangyo OF lipase; hepatic lipase; lipazin; post-heparin plasma protamine-resistant lipase; salt-resistant post-heparin lipase; heparin releasable hep | |
| Lysozyme from chicken egg white | Lysozyme from chicken egg white is a bactericidal enzyme, and it lyses gram-positive bacteria.Lysozyme from chicken egg white can also be used for the research of HIV infection and pulmonary emphysema. Group: Heterocyclic organic compound. CAS No. 12650-88-3. Appearance: Solid. Catalog: ACM12650883. | |
| MAleimido-3,5-disuccinimidyl isophthalate | MDSI is a cross-linker commonly used in bioconjugation reactions to covalently link proteins, peptides, and other biomolecules. MDSI is often used to develop novel biomaterials, such as hydrogels, which can be used in tissue engineering and drug delivery applications. MDSI is also used in biosensor development to immobilize enzymes and other biomolecules to the sensor surface. Group: Organic frame monomer block. Alternative Names: MDSI. CAS No. 1257094-24-8. Molecular formula: C20H13N3O10. Mole weight: 455.34 g/mol. Purity: 0.95. IUPACName: bis(2,5-dioxopyrrolidin-1-yl) 5-(2,5-dioxopyrrol-1-yl)benzene-1,3-dicarboxylate. Canonical SMILES: C1CC (=O)N (C1=O)OC (=O)C2=CC (=CC (=C2)N3C (=O)C=CC3=O)C (=O)ON4C (=O)CCC4=O. Catalog: ACM1257094248. | |
| Maltotriose | Maltotriose is a trisaccharide (three-part sugar) consisting of three glucose molecules linked with α-1,4 glycosidic bonds.It is most commonly produced by the digestive enzyme alpha-amylase (a common enzyme in human saliva) on amylose in starch. The creation of both maltotriose and maltose during this process is due to the random manner in which alpha amylase hydrolyses α-1,4 glycosidic bonds.It is the shortest chain oligosaccharide that can be classified as maltodextrin. Group: Heterocyclic organic compound. Alternative Names: 4-O-[4-O-(α-D-Glucopyranosyl)-α-D-glucopyranosyl]-D-glucose. CAS No. 1109-28-0. Molecular formula: C18H32O16. Mole weight: 504.44. Appearance: White to off-white powder. Purity: 0.98. IUPACName: (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-4,5-Dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol. Canonical SMILES: C (C1C (C (C (C (O1)OC2C (OC (C (C2O)O)OC3C (OC (C (C3O)O)O)CO)CO)O)O)O)O. Density: 1.4403 g/cm³. ECNumber: 214-174-2;232-945-1. Catalog: ACM1109280. | |
| manganese peroxidase | A hemoprotein. The enzyme from white rot basidiomycetes is involved in the oxidative degradation of lignin. The enzyme oxidizes a bound Mn2+ ion to Mn3+ in the presence of hydrogen peroxide. The product, Mn3+, is released from the active site in the presence of a chelator (mostly oxalate and malate) that stabilizes it against disproportionation to Mn2+ and insoluble Mn4+. The complexed Mn3+ ion can diffuse into the lignified cell wall, where it oxidizes phenolic components of lignin and other organic substrates. It is inactive with veratryl alcohol or nonphenolic substrates. Group: Enzymes. Synonyms: peroxidase-M2; Mn-dependent (NADH-oxidizing) peroxidase. Enzyme Commission Number: EC 1.11.1.13. CAS No. 114995-15-2. MnP. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0494; manganese peroxidase; EC 1.11.1.13; 114995-15-2; peroxidase-M2; Mn-dependent (NADH-oxidizing) peroxidase. Cat No: EXWM-0494. | |
| Methanol-d | Isotope labelled Methanol (M276585), which is a common chemical reagent in organic synthesis participating in a variety of reactions. Used to prepare novel triazole-polyphenol hybrid compounds as FabG4 (Rv0242c) enzyme inhibitors for the treatment of Mycobacterium Tuberculosis (1). Also used in the synthesis of prodelphinidin B1/B2/B4 which display antitumor activities against prostate cancer cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 1455-13-6. Pack Sizes: 10g, 25 g. Molecular Formula: CH3DO, Molecular Weight: 33.0499999999999. US Biological Life Sciences. | Worldwide |
| Methoxatin disodium salt | Methoxatin disodium salt. Applications: An organic enzyme cofactor. Group: Coenzymes. Synonyms: Pyrrolo-quinoline-quinone disodium salt; PQQ. CAS No. 122628-50-6. Purity: ≥97%. Mole weight: 374.17. Pyrrolo-quinoline-quinone disodium salt; PQQ; Methoxatin disodium salt; 122628-50-6. Cat No: COEC-078. | |
| Methyl Alcohol, 99+% | Methyl Alcohol is a common chemical reagent in organic synthesis participating in a variety of reactions. Used to prepare novel triazole-polyphenol hybrid compounds as FabG4 (Rv0242c) enzyme inhibitors for the treatment of Mycobacterium Tuberculosis (1). Also used in the synthesis of prodelphinidin B1/B2/B4 which display antitumor activities against prostate cancer cells.Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants. Group: Biochemicals. Alternative Names: Methanol; Bieleski's Solution; Carbinol; Methanol Cluster; Methyl Hydroxide; Methylol; Monohydroxymethane; NSC 85232; Wood Alcohol; MeOH, Hydroxymethane. Grades: Reagent Grade. CAS No. 67-56-1. Pack Sizes: 1L, 4L, 16L, 64L, 180L. Molecular Formula: CH3OH, Molecular Weight: 32.04. US Biological Life Sciences. | Worldwide |
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